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6β-fluoro-17β-hydroxy-4-androsten-3-one | 1852-58-0

中文名称
——
中文别名
——
英文名称
6β-fluoro-17β-hydroxy-4-androsten-3-one
英文别名
6β-fluoro-4-androsten-17β-ol-3-one;6β-fluoro-17β-hydroxy-androst-4-en-3-one;6β-Fluor-17β-hydroxy-androst-4-en-3-on;(6β,17β)-6-fluoro-17-hydroxy-androst-4-en-3-one;6|A-fluoro-17|A-hydroxyandrost-4-en-3-one;(6R,8R,9S,10R,13S,14S,17S)-6-fluoro-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
6β-fluoro-17β-hydroxy-4-androsten-3-one化学式
CAS
1852-58-0
化学式
C19H27FO2
mdl
——
分子量
306.421
InChiKey
GGQPTOITOZXLBE-ZVBLRVHNSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    22
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.84
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    卤代类固醇激素的合成—Ⅱ
    摘要:
    用三氟化硼醚化物在胆甾烷,雄烷酮和孕烷系列中裂解3β-乙酰氧基-5α-,6α-环氧化合物,得到相应的3β-乙酰氧基-5α-羟基-6β-氟代化合物。通过适当地操作这些氟代醇,可制得6α-氟胆甾烯酮和具有生物学意义的6α-和6β-氟睾酮以及6α-6β-氟孕酮。
    DOI:
    10.1016/s0040-4020(01)82606-5
  • 作为产物:
    描述:
    3β,17β-diacetoxy-6β-fluoro-androst-4-ene 在 manganese(IV) oxide 、 lithium aluminium tetrahydride 作用下, 生成 6β-fluoro-17β-hydroxy-4-androsten-3-one
    参考文献:
    名称:
    卤代类固醇激素的合成—Ⅱ
    摘要:
    用三氟化硼醚化物在胆甾烷,雄烷酮和孕烷系列中裂解3β-乙酰氧基-5α-,6α-环氧化合物,得到相应的3β-乙酰氧基-5α-羟基-6β-氟代化合物。通过适当地操作这些氟代醇,可制得6α-氟胆甾烯酮和具有生物学意义的6α-和6β-氟睾酮以及6α-6β-氟孕酮。
    DOI:
    10.1016/s0040-4020(01)82606-5
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文献信息

  • Power- and structure-variable fluorinating agents. The N-fluoropyridinium salt system
    作者:Teruo Umemoto、Shinji Fukami、Ginjiro Tomizawa、Kikuko Harasawa、Kosuke Kawada、Kyoichi Tomita
    DOI:10.1021/ja00179a047
    日期:1990.11
    N-Fluoropyridinium salts provide a new system of fluorinating agents by which a wide range of nucleophilic substrates differing in reactivity can be fluorinated due to the varying degree of fluorinating power and also fluorinated very selectively through structural alteration. The scope of selective fluorination should be broadened considerably on the basis of the present results. The N-fluoropyridinium
    N-氟吡啶鎓盐提供了一种新的氟化剂系统,通过该系统,由于氟化能力的不同程度,反应性不同的各种亲核底物可以被氟化,并且还可以通过结构改变非常有选择性地氟化。在现有结果的基础上,选择性氟化的范围应该大大拓宽。因此,N-氟吡啶鎓盐系统应该可以制备许多有用的有机氟化合物
  • Synthesis of C-6 fluoroandrogens: Evaluation of ligands for tumor receptor imaging
    作者:Yearn Seong Choe、John A. Katzenellenbogen
    DOI:10.1016/0039-128x(95)00009-f
    日期:1995.5
    Seven androgens, substituted with fluorine at C-6, were prepared as potential imaging agents for androgen receptor-positive prostate tumors and were evaluated in vitro in terms of their lipophilicity and their relative binding affinities (RBA, relative to R 1881 = 100) for the androgen receptor and for sex steroid binding protein. Introduction of a fluorine atom into the C-6 position of an androgen generally decreases binding affinity to the androgen receptor, except in the two cases: 6 alpha-fluoro-19-nor-testosterone (RBA = 41.6 versus 30.6 for the unsubstituted steroid) and 6 alpha-fluoro-19-nor-testosterone (RBA = 8.9 versus 6.6). Receptor binding of the C-6 fluoro-androgens is also stereospecific, showing higher binding affinities for the alpha-epimers compared to the corresponding beta-epimers (4:1-15:1). Binding affinity to sex steroid binding protein is the lowest with 19-nor-testosterone, which is also the least lipophilic androgen studied. Based on the binding properties of compounds in this series, 6 alpha-fluoro-19-nor-testosterone appears to have the most promise as a turner imaging agent.
  • Synthesis of halogenated steroid hormones—II
    作者:A. Bowers、H.J. Ringold
    DOI:10.1016/s0040-4020(01)82606-5
    日期:1958.1
    Fission of 3β-acetoxy-5α-,6α-epoxides in the cholestane, androstane and pregnane series with boron trifluoride etherate afforded the corresponding 3β-acetoxy-5α-hydroxy-6β-fluoro compounds. By appropriate manipulation of these fluorohydrins 6α-fluorocholestenone and the biologically interesting 6α- and 6β-fluorotestosterone and 6α- 6β-fluoroprogesterone were prepared.
    用三氟化硼醚化物在胆甾烷,雄烷酮和孕烷系列中裂解3β-乙酰氧基-5α-,6α-环氧化合物,得到相应的3β-乙酰氧基-5α-羟基-6β-氟代化合物。通过适当地操作这些氟代醇,可制得6α-氟胆甾烯酮和具有生物学意义的6α-和6β-氟睾酮以及6α-6β-氟孕酮。
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